Role of CD248 as a potential severity marker in idiopathic pulmonary fibrosis. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Bartis, Domokos; Crowley, Louise; D'Souza, Vijay; Borthwick, Lee; Fisher, Andrew; Croft, Adam; Pongrácz, Judit; Thompson, Richard; Langman, Gerald; Buckley, Christopher; Thickett, David
• Is Part Of: BMC pulmonary medicine. Volume 16:Issue 1(2016)
• Page Start: 1
• Page End: 10
• Publication Date: 2016-12
• Subjects: IPF -- Idiopathic pulmonary fibrosis -- TGF-beta -- CD248 -- Endosialin -- Biomarker; Lungs -- Diseases -- Periodicals; 616.24005
• DOI: 10.1186/s12890-016-0211-7
• Languages: English
• ISSNs: 1471-2466

Abstract

Abstract Background CD248 or Endosialin is a transmembrane molecule expressed in stromal cells binding to extracellular matrix (ECM) components. It has been previously implicated in kidney fibrosis, rheumatoid arthritis as well as in tumour-stromal interactions. This study investigates the role of CD248 in the pathogenesis of fibrotic diseases in Idiopathic Pulmonary Fibrosis (IPF). Methods CD248 quantitative immunohistochemistry (IHC) was performed on lung samples from 22 IPF patients and its expression was assayed in cultured pulmonary fibroblasts and epithelial cells. Effects of CD248 silencing was evaluated on fibroblast proliferation and myofibroblast differentiation. Results IHC revealed strong CD248 expression in mesenchymal cells of normal lung structures such as pleura and adventitia but not in epithelium. Fibrotic areas showed markedly stronger staining than unaffected lung tissue. The extent of CD248 staining showed a significant negative correlation to lung function parameters FEV1, FVC, TLC, and TLCO (r2 > 0 · 35, p < 0 · 01). CD248 protein levels were significantly greater in IPF-derived lung fibroblasts vs normal lung fibroblasts (p < 0 · 01) and CD248 silencing significantly reduced the proliferation of lung fibroblasts, but did not affected myofibroblast differentiation. Conclusion We conclude that CD248 overexpression is possibly involved in the pathogenesis of IPF and it has potential as a disease severity marker. Given that CD248 ligands are collagen type I, IV and fibronectin, we hypothesise that CD248 signalling represents a novel matrix-fibroblast interaction that may be a potential therapeutic target in IPF.